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The Glucocorticoid axis
Reem Alyahya
Introduction
• A 46 y/o man present with fever, red
tender area on his right leg, consistent
with erysipelas.
• His recent medical history reveals
fatigue, easy bruising and wt. gain in the
past 6 months.
• His family history is negative for DM and
HT.
• physical examination shows central
obesity (BMI 32.5 kg/m2, waist
circumference 115 cm)
• BP 160/104
• Moon face appearance, a dorsal fat pad
in the neck and abdominal purple striae.
Learning objectives:
• Which additional radiological investigations do you recommend?
• Which treatment would you propose?
What is Cushing’s syndrome?
• Cushing syndrome is caused by prolonged exposure to elevated levels of
either endogenous glucocorticoids or exogenous glucocorticoids.
endogenous
• glucocorticoid
overproduction
or
hypercortisolism
• Due to primary
adrenocortical
neoplasm
exogenous
• Following the
therapeutic
adminstrition of
synthetic
steroids of
ACTH.
Cushing’s syndrome VS Cushing’s disease ?
• Cushing’s syndrome :
- clinical state of increased free
circulating glucocorticoid
- Spontaneous Cushing’s
syndrome rare
• Cushing’s Disease:
- ACTH dependent
hypercorticism , pituitary
dependant.
- it is the most common cause of
Cushing's.
Radiological investigations
Radiological investigations
 It should be performed after the biochemical laboratory evaluation has
been done.
 It’s used to determine the cause or complications.
Adrenal CT or
MRI
Pituitary MRI Chest X-ray
Radiolabelled
octreotide
(Scintigraphy)
Adrenal CT or MRI:
• Adrenal adenomas and
carcinomas are relatively large
and can be detected by CT scan
imaging.
Pituitary MRI
• A pituitary adenoma can be seen
but it is often small and not
visible in a significant proportion
of cases.
Chest X-ray
• It is used in patients with
suspected ectopic ACTH
production.
• The ACTH-secreting tumors are
often oat-cell carcinomas of the
lung (bronchus carcinoma).
Radiolabelled octreotide
(Scintigraphy)
• involves injection of a radioactive
substance followed by an imaging
scan.
• Occasionally used in locating
ectopic ACTH tumors.
Treatment
• Successful treatment of Cushing’s syndrome should lead to reversal of the
presenting clinical features.
• However, untreated Cushing’s syndrome has a very bad prognosis, with
death from: hypertension, MI, infection and heart failure.
• Whatever the underlying cause, cortisol hypersecretion should be
controlled prior to surgery or radiotherapy.
pharmacotherapy
Surgery
Radiotherapy
Depending
on the
cause.
Pharmacotherapy (Cushing’s syndrome)
• The goal of pharmacotherapy is to reduce morbidity and prevent
complications.
Somatostatin
Analogs
• bind and activate human
somatostatin receptors
resulting in inhibition of
ACTH secretion, which
leads to decreased
cortisol secretion.
• pasireotide
0.6-0.9 twice daily
Adrenal steroid
inhibitors
• These agents either
inhibit the synthesis of
mineralocorticoids and
glucocorticoids, or
competitively bind
glucocorticoid receptors.
• Metyrapone
750 mg – 4 g daily , in 3-4
divided doses.
• Ketoconazole :200 mg
three times daily
Surgery and radiotherapy (Cushing’s disease)
Trans-sphenoidal
removal of the
tumor.
Bilateral
adrenalectomy
Pituitary
irradiation
Trans-sphenoidal removal of the tumor
• Is the treatment of choice.
• Result in remission of 75-80% of
the cases.
• But the results vary considerably.
• Experienced surgeon is essential.
Bilateral adrenalectomy
• It’s an effective last resort if other
measures fail to control the
disease.
• The patient will need
hydrocortisone (cortisol)
replacement therapy after
surgery, and possibly continued
throughout life.
Radiotherapy (pituitary irrdiation).
• Alone is slow acting.
• Only effective in 50-60% even
after prolonged follow up
• Used mainly after failed pituitary
surgery.
Cushing’s syndrome due to other causes.
 Adrenal adenomas:
- should be resected after
achievement of clinical remission
with metyrapone.
 Adrenal carcinoma:
- are highly aggressive and has
poor prognosis.
- if there’s no widespread
metastases, tumor bulk should be
removed surgically.
- adrenolytic drug mitotane may
inhibit the growth of the tumor
and prolonged survival.
- radiotherapy can be used.
conclusion
• A 46 y/o man present with fatigue, easy bruising and wt. gain
• The patient had moon face appearance, a dorsal fat pad in the neck and
abdominal purple striae.
• The diagnostic tests reveals that the patient has Cushing's syndrome.
• The patient will initially manage the cortisol levels by taking metyrapone
4 gm/ 3 daily, Ketoconazole, 200 mg /3 daily
• Further treatment decided based on the specific etiology.
References
• Kumar & Clarks, Clinical Medicine ,
eighth edition (2012).
• Up to date : Cushing's syndrome.
• Up to date : Cushing's syndrome
treatment (Beyond the Basics)
• Emedicine : medscape: Cushing’s
syndrome.
Thank you for listening.
Any question?

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cushing syndrome-5.pdf

  • 2. Introduction • A 46 y/o man present with fever, red tender area on his right leg, consistent with erysipelas. • His recent medical history reveals fatigue, easy bruising and wt. gain in the past 6 months. • His family history is negative for DM and HT. • physical examination shows central obesity (BMI 32.5 kg/m2, waist circumference 115 cm) • BP 160/104 • Moon face appearance, a dorsal fat pad in the neck and abdominal purple striae.
  • 3. Learning objectives: • Which additional radiological investigations do you recommend? • Which treatment would you propose?
  • 4. What is Cushing’s syndrome? • Cushing syndrome is caused by prolonged exposure to elevated levels of either endogenous glucocorticoids or exogenous glucocorticoids. endogenous • glucocorticoid overproduction or hypercortisolism • Due to primary adrenocortical neoplasm exogenous • Following the therapeutic adminstrition of synthetic steroids of ACTH.
  • 5. Cushing’s syndrome VS Cushing’s disease ? • Cushing’s syndrome : - clinical state of increased free circulating glucocorticoid - Spontaneous Cushing’s syndrome rare • Cushing’s Disease: - ACTH dependent hypercorticism , pituitary dependant. - it is the most common cause of Cushing's.
  • 7. Radiological investigations  It should be performed after the biochemical laboratory evaluation has been done.  It’s used to determine the cause or complications. Adrenal CT or MRI Pituitary MRI Chest X-ray Radiolabelled octreotide (Scintigraphy)
  • 8. Adrenal CT or MRI: • Adrenal adenomas and carcinomas are relatively large and can be detected by CT scan imaging.
  • 9. Pituitary MRI • A pituitary adenoma can be seen but it is often small and not visible in a significant proportion of cases.
  • 10. Chest X-ray • It is used in patients with suspected ectopic ACTH production. • The ACTH-secreting tumors are often oat-cell carcinomas of the lung (bronchus carcinoma).
  • 11. Radiolabelled octreotide (Scintigraphy) • involves injection of a radioactive substance followed by an imaging scan. • Occasionally used in locating ectopic ACTH tumors.
  • 12. Treatment • Successful treatment of Cushing’s syndrome should lead to reversal of the presenting clinical features. • However, untreated Cushing’s syndrome has a very bad prognosis, with death from: hypertension, MI, infection and heart failure. • Whatever the underlying cause, cortisol hypersecretion should be controlled prior to surgery or radiotherapy.
  • 14. Pharmacotherapy (Cushing’s syndrome) • The goal of pharmacotherapy is to reduce morbidity and prevent complications. Somatostatin Analogs • bind and activate human somatostatin receptors resulting in inhibition of ACTH secretion, which leads to decreased cortisol secretion. • pasireotide 0.6-0.9 twice daily Adrenal steroid inhibitors • These agents either inhibit the synthesis of mineralocorticoids and glucocorticoids, or competitively bind glucocorticoid receptors. • Metyrapone 750 mg – 4 g daily , in 3-4 divided doses. • Ketoconazole :200 mg three times daily
  • 15. Surgery and radiotherapy (Cushing’s disease) Trans-sphenoidal removal of the tumor. Bilateral adrenalectomy Pituitary irradiation
  • 16. Trans-sphenoidal removal of the tumor • Is the treatment of choice. • Result in remission of 75-80% of the cases. • But the results vary considerably. • Experienced surgeon is essential.
  • 17. Bilateral adrenalectomy • It’s an effective last resort if other measures fail to control the disease. • The patient will need hydrocortisone (cortisol) replacement therapy after surgery, and possibly continued throughout life.
  • 18. Radiotherapy (pituitary irrdiation). • Alone is slow acting. • Only effective in 50-60% even after prolonged follow up • Used mainly after failed pituitary surgery.
  • 19. Cushing’s syndrome due to other causes.  Adrenal adenomas: - should be resected after achievement of clinical remission with metyrapone.  Adrenal carcinoma: - are highly aggressive and has poor prognosis. - if there’s no widespread metastases, tumor bulk should be removed surgically. - adrenolytic drug mitotane may inhibit the growth of the tumor and prolonged survival. - radiotherapy can be used.
  • 20. conclusion • A 46 y/o man present with fatigue, easy bruising and wt. gain • The patient had moon face appearance, a dorsal fat pad in the neck and abdominal purple striae. • The diagnostic tests reveals that the patient has Cushing's syndrome. • The patient will initially manage the cortisol levels by taking metyrapone 4 gm/ 3 daily, Ketoconazole, 200 mg /3 daily • Further treatment decided based on the specific etiology.
  • 21. References • Kumar & Clarks, Clinical Medicine , eighth edition (2012). • Up to date : Cushing's syndrome. • Up to date : Cushing's syndrome treatment (Beyond the Basics) • Emedicine : medscape: Cushing’s syndrome.
  • 22. Thank you for listening. Any question?